L-Histidine trials recruiting now

6 registrations that name L-Histidine as a study arm and are recruiting or about to, as ClinicalTrials.gov listed them on Oct 20, 2026. Read each listing for its full criteria and current status.

Kymata never assesses eligibility. Each listing names its own criteria; only its study team can say whether someone can join. Trial doses are given under the trial's monitoring and are not a schedule for anyone outside it.

Filter 6 registrations

Status

Phase

8US sites across 6 states

All 6 registrations

RecruitingNCT02947750

Neurovascular Transduction During Exercise in Chronic Kidney Disease

  • Phase 2
  • Emory University
  • About 150 people
  • Started Oct 2016

In plain words A Phase 2 study of L-Histidine in people 18 to 75, run by Emory University. It plans to enroll about 150 people at 3 US sites.

Who it lists and where

Who the trial lists, as registered

Lists people 18 to 75. Conditions: Renal Insufficiency, Chronic.

  • Stage III or IV Chronic Kidney Disease, defined as reduction in estimated glomerular filtration rate (eGFR) to 15-59 cc/minute as calculated by the modified Modification of Diet in Renal Disease (MDRD) Study equation or the Chronic Kidney…
  • Stable renal function, with no greater than a 30% reduction in eGFR over the prior 3 months
  • Does not exercise regularly (defined as exercising less than 20 minutes twice per week)
  • Willing and able to cooperate with the study protocol

2 more inclusion criteria and the exclusion criteria are on the listing.

What it tests, as registered

6R-BH4; 6R-BH4 placebo; Folic acid; Exercise training; Stretching; Histidine and beta-alanine supplementation; Histidine and beta-alanine placebo

Registered summary

The purpose of this study is to find out why patients with chronic kidney disease (CKD) have poor exercise capacity and to explore what causes an increase in blood pressure during exercise (i.e. increased adrenaline levels, or decreased ability of blood vessels to dilate). This study will also test whether or not regular exercise on a bicycle and/or treatment with 6R-BH4 (Kuvan) pills, or histidine and beta-alanine supplementation improves these measures during exercise. The full summary is on the listing.

Where, as registered

3 US sites in 1 state.

RecruitingNCT06050668

Essential Amino Acid Supplementation for Femoral Fragility Fractures

  • Phase 2
  • Michael C Willey
  • About 60 people
  • Started Jun 17, 2024

In plain words A Phase 2 study of L-Histidine in people 65 and older, run by Michael C Willey. It plans to enroll about 60 people at 2 US sites.

Who it lists and where

Who the trial lists, as registered

Lists people 65 and older. Conditions: Femoral Fracture; Fragility Fracture; Muscle Atrophy.

  • Hospital inpatient
  • Age ≥ 65 years old on admission
  • Low-energy mechanism of injury
  • Diagnosis of femur fracture (OTA 31, 32, or 33 fracture)

2 more inclusion criteria and the exclusion criteria are on the listing.

What it tests, as registered

Essential Amino Acid Supplementation

Registered summary

This trial will evaluate the impact of 4 weeks of postoperative essential amino acid (EAA)-based supplementation on muscle morphology after femoral fragility fracture. This trial will assess the ability of EAA-based to increase skeletal muscle metabolic activity, reduce inflammation, and induce muscle fiber hypertrophy, as well as preserve skeletal muscle mass and physical performance up to 6 months after injury. Participants will be randomized in a 1:1 ratio to 1) standard of care (no dietary intervention) or 2) EAA-based supplementation.

Where, as registered

2 US sites in 2 states.

RecruitingNCT07792603

Daily Upgrade Trial

  • No phase
  • University of North Carolina, Chapel Hill
  • About 44 people
  • Started Aug 31, 2026

In plain words A study of L-Histidine in female participants 25 to 45, run by University of North Carolina, Chapel Hill. It plans to enroll about 44 people at 1 US site.

Who it lists and where

Who the trial lists, as registered

Lists female participants 25 to 45; healthy volunteers accepted. Conditions: Healthy Women.

  • Participant is an adult between the ages of 25-45 years
  • Participant has a recorded BMI between 18.5-30 kg/m\^2
  • Participant is apparently healthy and free from disease, as determined by a health history questionnaire
  • Participant is a biological female

4 more inclusion criteria and the exclusion criteria are on the listing.

What it tests, as registered

Essential Amino Acid+; Non-Calorie Placebo; High intensity Interval Training; No Exercise

Registered summary

This study evaluates the acute and chronic effects of an essential amino acid supplement (Daily Upgrade EAA+) on metabolomics, amino acid kinetics, metabolic rate, body composition in active adult women. The study consists of an acute randomized double-blind crossover phase comparing EAA+, whey protein isolate, and placebo before high-intensity interval training (HIIT), and a chronic randomized double-blind parallel-arm phase evaluating 3 weeks of EAA+ or placebo supplementation combined with twice-weekly HIIT.

Where, as registered

1 US site in 1 state.

RecruitingNCT03208868

Leucine Enriched Essential Amino Acid Mixture to Reverse Muscle Loss in Cirrhosis

  • No phase
  • The Cleveland Clinic
  • About 32 people
  • Started Aug 5, 2013

In plain words A study of L-Histidine in people 18 to 70, run by The Cleveland Clinic. It plans to enroll about 32 people at 1 US site.

Who it lists and where

Who the trial lists, as registered

Lists people 18 to 70; healthy volunteers accepted. Conditions: Cirrhosis, Liver.

  • Cirrhotic patients:
  • Cirrhosis diagnosed by liver biopsy and/or clinical, biochemical and imaging evidence of cirrhosis.
  • Abstinence from alcohol and/or other recreational drugs for at least 6 months
  • Child's Pugh score 5-9 (inclusive).

11 more inclusion criteria and the exclusion criteria are on the listing.

What it tests, as registered

Leucine enriched essential amino acid (EEA/LEU); Balanced amino acid supplement (BAA)

Registered summary

Loss of skeletal muscle mass or sarcopenia is the most common and potentially reversible complication in cirrhosis that increases morbidity and mortality before, during and after liver transplantation. No proven treatments exist for the prevention or reversal of sarcopenia in cirrhosis, primarily because the mechanisms responsible for this are unknown. The full summary is on the listing.

Where, as registered

1 US site in 1 state.

RecruitingNCT07577505

Histidine Supplementation for Antitumor Immunity in Colorectal Cancer

  • No phase
  • Jing-yuan Fang, MD, Ph. D
  • About 20 people
  • Started May 6, 2026

In plain words A study of L-Histidine in people 18 to 80, run by Jing-yuan Fang, MD, Ph. D. It plans to enroll about 20 people at 1 site, none in the US.

Who it lists and where

Who the trial lists, as registered

Lists people 18 to 80. Conditions: Colorectal Cancer.

  • Patients aged 18-80 years, regardless of sex.
  • Body mass index (BMI) ≥18.5.
  • NRS-2002 score <3.
  • Diagnosed with stage II or higher colorectal cancer who require pharmacological intervention.

2 more inclusion criteria and the exclusion criteria are on the listing.

What it tests, as registered

Histidine

Registered summary

The goal of this clinical study is to learn whether oral histidine supplementation may be safely used to support antitumor immune function during standard colorectal cancer treatment. Participants with colorectal cancer in the supplementation group will: Take 2g oral histidine once daily during standard colorectal cancer treatment; Provide blood samples before and after supplementation; Attend regular follow-up visits for laboratory tests, safety assessment, and treatment evaluation.

Where, as registered

No US site; China (1).

Not yet recruitingNCT07700368

Effect of Monosodium Glutamate on Microbiome-Derived Imidazole Propionate Production in Healthy Volunteers

  • No phase
  • University of Chicago
  • About 18 people
  • Starts Jul 15, 2026 (estimated)

In plain words A study of L-Histidine in people 18 and older, run by University of Chicago. It plans to enroll about 18 people at 1 US site.

Who it lists and where

Who the trial lists, as registered

Lists people 18 and older; healthy volunteers accepted. Conditions: Healthy Adult.

  • Age 18 years or older
  • No antibiotic use in the previous 3 months

The exclusion criteria are on the listing.

What it tests, as registered

L-histidine; Monosodium glutamate (MSG); Sodium chloride (NaCl)

Registered summary

The goal of this clinical trial is to learn whether dietary monosodium glutamate (MSG), a common food flavor enhancer, increases the blood level of a gut-microbiome-derived compound called imidazole propionate (ImP) in healthy adult volunteers. ImP is a compound made by gut bacteria from the amino acid histidine, and higher blood levels have been linked to problems with blood-sugar control. The full summary is on the listing.

Where, as registered

1 US site in 1 state.

ClinicalTrials.gov lists 102 open registrations for this search, including ones where L-Histidine is not a study arm or that are past the 6 we keep. Search them on ClinicalTrials.gov (opens in new tab).

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